| Literature DB >> 33090806 |
Farah Benyettou1, Gobinda Das1, Anjana Ramdas Nair1, Thirumurugan Prakasam1, Digambar B Shinde2, Sudhir Kumar Sharma1, Jamie Whelan1, Yoann Lalatonne3,4, Hassan Traboulsi5, Renu Pasricha1, Osama Abdullah1, Ramesh Jagannathan1, Zhiping Lai2, Laurence Motte6, Felipe Gándara7, Kirsten C Sadler1, Ali Trabolsi1.
Abstract
Nanoscale imine-linked covalent organic frameworks (nCOFs) were first loaded with the anticancer drug Doxorubicin (Dox), coated with magnetic iron oxide nanoparticles (γ-Fe2O3 NPs), and stabilized with a shell of poly(l-lysine) cationic polymer (PLL) for simultaneous synergistic thermo-chemotherapy treatment and MRI imaging. The pH responsivity of the resulting nanoagents (γ-SD/PLL) allowed the release of the drug selectively within the acidic microenvironment of late endosomes and lysosomes of cancer cells (pH 5.4) and not in physiological conditions (pH 7.4). γ-SD/PLL could efficiently generate high heat (48 °C) upon exposure to an alternating magnetic field due to the nCOF porous structure that facilitates the heat conduction, making γ-SD/PLL excellent heat mediators in an aqueous solution. The drug-loaded magnetic nCOF composites were cytotoxic due to the synergistic toxicity of Dox and the effects of hyperthermia in vitro on glioblastoma U251-MG cells and in vivo on zebrafish embryos, but they were not significantly toxic to noncancerous cells (HEK293). To the best of our knowledge, this is the first report of multimodal MRI probe and chemo-thermotherapeutic magnetic nCOF composites.Entities:
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Year: 2020 PMID: 33090806 DOI: 10.1021/jacs.0c05381
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419